| human | Q5 |
| P2013 | Facebook username | martin.smith |
| P2037 | GitHub username | ms609 |
| P6634 | LinkedIn personal profile ID | ms609 |
| P496 | ORCID iD | 0000-0001-5660-1727 |
| P3829 | Publons author ID | 1313384 |
| P1053 | ResearcherID | B-8461-2012 |
| P1153 | Scopus author ID | 15037387100 |
| P2002 | X username | PalaeoSmith |
| P69 | educated at | University of Cambridge | Q35794 |
| University of Toronto | Q180865 | ||
| P108 | employer | Durham University | Q458393 |
| P734 | family name | Smith | Q1158446 |
| Smith | Q1158446 | ||
| Smith | Q1158446 | ||
| P735 | given name | Martin | Q18002399 |
| Martin | Q18002399 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q54005281 | A new view onNematothallus: coralline red algae from the Silurian of Gotland |
| Q54005245 | A palaeoscolecid worm from the Burgess Shale |
| Q104452949 | An Ordovician nectocaridid hints at an endocochleate origin of Cephalopoda |
| Q64948677 | An algorithm for Morphological Phylogenetic Analysis with Inapplicable Data. |
| Q24568333 | Articulated Wiwaxia from the Cambrian Stage 3 Xiaoshiba lagerstätte |
| Q54005318 | Batteries versus biomass as a transport solution |
| Q92923407 | Bayesian and parsimony approaches reconstruct informative trees from simulated morphological datasets |
| Q28686913 | Beyond the Burgess Shale: Cambrian microfossils track the rise and fall of hallucigeniid lobopodians |
| Q54005304 | Comment on the "Hypothesis for the role of toxin-producing algae in Phanerozoic mass extinctions based on evidence from the geologic record and modern environments" (Discussion) |
| Q92651873 | Congruence, fossils and the evolutionary tree of rodents and lagomorphs |
| Q54005238 | Cord-forming Palaeozoic fungi in terrestrial assemblages |
| Q46479297 | Evolution: Velvet Worm Biogeography |
| Q54005268 | First report of Wiwaxia from the Cambrian Chengjiang Lagerstätte |
| Q34482087 | Hallucigenia's head and the pharyngeal armature of early ecdysozoans |
| Q34434025 | Hallucigenia's onychophoran-like claws and the case for Tactopoda |
| Q36246912 | Hyoliths are Palaeozoic lophophorates |
| Q57211856 | Hyoliths with pedicles illuminate the origin of the brachiopod body plan |
| Q54005297 | Likelihood and parsimony diverge at high taxonomic levels |
| Q54005200 | Morphological phylogenetic analysis with inapplicable data |
| Q28273558 | Mouthparts of the Burgess Shale fossils Odontogriphus and Wiwaxia: implications for the ancestral molluscan radula |
| Q54005285 | Nectocaridid ecology, diversity, and affinity: early origin of a cephalopod-like body plan |
| Q54005310 | Nectocaris and early cephalopod evolution: reply to Mazurek & Zatoń |
| Q28606721 | New reconstruction of the Wiwaxia scleritome, with data from Chengjiang juveniles |
| Q54005276 | Ontogeny, morphology and taxonomy of the soft-bodied Cambrian ‘mollusc’Wiwaxia |
| Q31133450 | Onychophoran-like musculature in a phosphatized Cambrian lobopodian |
| Q46254126 | Orthrozanclus elongata n. sp. and the significance of sclerite-covered taxa for early trochozoan evolution |
| Q34117622 | Primitive soft-bodied cephalopods from the Cambrian |
| Q54005250 | Sclerites and possible mouthparts ofWiwaxiafrom the temperate palaeolatitudes of Colombia, South America |
| Q54005259 | The macro- and microfossil record of the Cambrian priapulidOttoia |
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